Preparation and cyclization of 4-chloro-5,5-dimethyl-3-formyl-1,2-oxathiolene 2,2-dioxide
β Scribed by Li Tian; Lun-Zu Liu
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 100 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20094
No coin nor oath required. For personal study only.
β¦ Synopsis
Chloroformylation of 5,5-dimethyl-1,2- oxathiolan-4-one 2,2-dioxide 4 with Vilsmeier reagent (DMF/POCl 3 ) led to the formation of cyclic Ξ²-chlorovinylaldehyde (4-chloro-5,5-dimethyl-3-formyl-1,2oxathiolene 2,2-dioxide 5). Compound 5 reacted with formamidine, o-aminophenol, 1,2-phenylenediamine, aminopyrazole, and aminotetrazole to give the corresponding heterocyclic compounds.
π SIMILAR VOLUMES
**Synthesis of 5,6βDimethylβ4βoxoβ1,3,4,5βtetrahydroβimidazo[4,5β__c__][1,2,6]thiadiazin 2,2βdioxide and 7βMethylβ4βoxoβ1__H__β3,4βdihydropyrimido[4,5β__c__][1,2,6]thiadiazin 2,2βdioxide** The derivatives of the above heterocyclic ring systems were prepared by reaction of the corresponding __o__βam